Variant report

Variant rs1197676
Chromosome Location chr15:42168018-42168019
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:42138200-42173400 Weak transcription Right Atrium heart
2 chr15:42141200-42191200 Weak transcription Aorta Aorta
3 chr15:42148200-42174400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr15:42153200-42168600 Strong transcription Breast Myoepithelial Primary Cells Breast
5 chr15:42155800-42168400 Weak transcription Lung lung
6 chr15:42157400-42179200 Weak transcription HSMMtube muscle
7 chr15:42159400-42168800 Weak transcription Fetal Intestine Small intestine
8 chr15:42160200-42172600 Weak transcription HUVEC blood vessel
9 chr15:42162400-42168400 Weak transcription Gastric stomach
10 chr15:42163200-42174000 Weak transcription Placenta Amnion Placenta Amnion
11 chr15:42163400-42168200 Weak transcription Spleen Spleen
12 chr15:42163600-42169600 Weak transcription Esophagus oesophagus
13 chr15:42163600-42173000 Weak transcription HSMM muscle
14 chr15:42163800-42170000 Weak transcription Adipose Nuclei Adipose
15 chr15:42164600-42171800 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr15:42165400-42184800 Weak transcription HMEC breast
17 chr15:42165600-42169000 Weak transcription Pancreas Pancrea
18 chr15:42167400-42168600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
19 chr15:42167600-42168400 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
20 chr15:42167600-42168400 Weak transcription Fetal Muscle Leg muscle
21 chr15:42167800-42169200 Enhancers Primary B cells from peripheral blood blood
22 chr15:42168000-42168400 Enhancers Primary B cells from cord blood blood

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